Photostimulation of lymphatic clearance of β-amyloid from mouse brain: a new strategy for the therapy of Alzheimer’s disease
Dongyu Li, Hao Lin, Silin Sun, Shaojun Liu, Zhang Liu, Yuening He, Jingtan Zhu, Jianyi Xu, Oxana Semyachkina-Glushkovskaya, Tingting Yu, Dan Zhu
Photostimulation of lymphatic clearance of β-amyloid from mouse brain: a new strategy for the therapy of Alzheimer’s disease
Alzheimer’s disease (AD) is an age-related neurodegenerative disorder that poses a significant burden on socio-economic and healthcare systems worldwide. However, the currently available therapy of AD is limited, and new strategies are needed to enhance the clearance of β-amyloid (Aβ) protein and improve cognitive function. Photobiomodulation (PBM) is a noninvasive and effective therapeutic method that has shown promise in treating various brain diseases. Here, we demonstrate that 1267-nm PBM significantly alleviates cognitive decline in the 5xFAD mouse model of AD and is safe as it does not induce a significant increase in cortical temperature. Moreover, with the combination of 3D tissue optical clearing imaging and automatic brain region segmentation, we show that PBM-mediated reductions of Aβ plaques in different subregions of prefrontal cortex and the hippocampus are different. The PBM-induced lymphatic clearance of Aβ from the brain is associated with improvement of memory and cognitive functions in 5xFAD mice. Our results suggest that the modulation of meningeal lymphatic vessels (MLVs) should play an important role in promoting Aβ clearance. Collectively, this pilot study demonstrates that PBM can safely accelerate lymphatic clearance of Aβ from the brain of 5xFAD mice, promoting improvement of neurocognitive status of AD animals suggesting that PBM can be an effective and bedside therapy for AD.
Photostimulation / Meningeal lymphatic vessels / Amyloid-β clearance / Alzheimer’s disease
[1] |
Scheltens,P., De Strooper,B., Kivipelto,M., Holstege,H., Chételat,G., Teunissen,C.E., Cummings,J., van der Flier,W.M.: Alzheimer’s disease. Lancet 397 (10284), 1577- 1590 (2021)
|
[2] |
Hardy,J.A., Higgins,G.A.: Alzheimer’s disease: the amyloid cascade hypothesis. Science 256 (5054), 184- 185 (1992)
|
[3] |
Cheng,Y., Tian,D., Wang,Y.: Peripheral clearance of brainderived Aβ in Alzheimer’s disease: pathophysiology and therapeutic perspectives. Transl. Neurodegener. 9 (1), 16 (2020)
|
[4] |
Salehpour,F., Khademi,M., Bragin,D.E., DiDuro,J.O.: Photobiomodulation therapy and the glymphatic system: promising applications for augmenting the brain lymphatic drainage system. Int. J. Mol. Sci. 23 (6), 2975 (2022)
|
[5] |
Farivar,S., Malekshahabi,T., Shiari,R.: Biological effects of lowlevel laser therapy. J. Lasers. Med. Sci. 5 (2), 58- 62 (2014)
|
[6] |
Tao,L., Liu,Q., Zhang,F., Fu,Y., Zhu,X., Weng,X., Han,H., Huang,Y., Suo,Y., Chen,L., Gao,X., Wei,X.: Microglia modulation with 1070-nm light attenuates Aβ burden and cognitive impairment in Alzheimer’s disease mouse model. Light. Sci. Appl. 10 (1), 179 (2021)
|
[7] |
Li,Q., Peng,J., Luo,Y., Zhou,J., Li,T., Cao,L., Peng,S., Zuo,Z., Wang,Z.: Far infrared light irradiation enhances Aβ clearance via increased exocytotic microglial ATP and ameliorates cognitive deficit in Alzheimer’s disease-like mice. J. Neuroinflammation 19 (1), 145 (2022)
|
[8] |
Yang,L., Wu,C., Parker,E., Li,Y., Dong,Y., Tucker,L., Brann,D.W., Lin,H.W., Zhang,Q.: Non-invasive photobiomodulation treatment in an Alzheimer Disease-like transgenic rat model. Theranostics 12 (5), 2205- 2231 (2022)
|
[9] |
Zhang,Z., Shen,Q., Wu,X., Zhang,D., Xing,D.: Activation of PKA/SIRT1 signaling pathway by photobiomodulation therapy reduces Aβ levels in Alzheimer’s disease models. Aging Cell 19 (1), e13054 (2020)
|
[10] |
Yue,X., Mei,Y., Zhang,Y., Tong,Z., Cui,D., Yang,J., Wang,A., Wang,R., Fei,X., Ai,L., Di,Y., Luo,H., Li,H., Luo,W., Lu,Y., Li,R., Duan,C., Gao,G., Yang,H., Sun,B., He,R., Song,W., Han,H., Tong,Z.: New insight into Alzheimer’s disease: light reverses Aβ-obstructed interstitial fluid flow and ameliorates memory decline in APP/PS1 mice. Alzheimers Dement. 5, 671- 684 (2019)
|
[11] |
Da Mesquita,S., Papadopoulos,Z., Dykstra,T., Brase,L., Farias,F.G., Wall,M., Jiang,H., Kodira,C.D., de Lima,K.A., Herz,J., Louveau,A., Goldman,D.H., Salvador,A.F., Onengut-Gumuscu,S., Farber,E., Dabhi,N., Kennedy,T., Milam,M.G., Baker,W., Smirnov,I., Rich,S.S., Benitez,B.A., Karch,C.M., Perrin,R.J., Farlow,M., Chhatwal,J.P., Holtzman,D.M., Cruchaga,C., Harari,O., Kipnis,J., Dominantly Inherited Alzheimer N,: Meningeal lymphatics affect microglia responses and anti-Aβ immunotherapy. Nature593 (7858), 255- 260 (2021)
|
[12] |
Semyachkina-Glushkovskaya, O., Penzel,T., Blokhina,I., Khorovodov,A., Fedosov,I., Yu,T., Karandin,G., Evsukova,A., Elovenko,D., Adushkina,V., Shirokov,A., Dubrovskii,A., Terskov,A., Navolokin,N., Tzoy,M., Ageev,V., Agranovich,I., Telnova,V., Tsven,A., Kurths,J.: Night photostimulation of clearance of beta-amyloid from mouse brain: new strategies in preventing Alzheimer’s disease. Cells 10 (12), 3289 (2021)
|
[13] |
Zinchenko,E., Navolokin,N., Shirokov,A., Khlebtsov,B., Dubrovsky,A., Saranceva,E., Abdurashitov,A., Khorovodov,A., Terskov,A., Mamedova,A., Klimova,M., Agranovich,I., Martinov,D., Tuchin,V., Semyachkina-Glushkovskaya,O., Kurts,J.: Pilot study of transcranial photobiomodulation of lymphatic clearance of beta-amyloid from the mouse brain: breakthrough strategies for non-pharmacologic therapy of Alzheimer’s disease. Biomed. Opt. Express 10 (8), 4003- 4017 (2019)
|
[14] |
Oakley,H., Cole,S.L., Logan,S., Maus,E., Shao,P., Craft,J., Guillozet-Bongaarts,A., Ohno,M., Disterhoft,J., Eldik,L.V., Berry,R., Vassar,R.: Intraneuronal β-amyloid aggregates, neurodegeneration, and neuron loss in transgenic mice with five familial Alzheimer’s disease mutations: potential factors in amyloid plaque formation. J. Neurosci. 26 (40), 10129- 10140 (2006)
|
[15] |
Liu S., Li D., Yu T., Zhu J., Semyachkina-Glushkovskaya O., ZhuD.: Transcranial photobiomodulation improves insulin therapy in diabetic mice: modulation of microglia and the brain drainage system.
|
[16] |
Martorell,A.J., Paulson,A.L., Suk,H.J., Abdurrob,F., Drummond,G.T., Guan,W., Young,J.Z., Kim,D.N.W., Kritskiy,O., Barker,S.J., Mangena,V., Prince,S.M., Brown,E.N., Chung,K., Boyden,E.S., Singer,A.C., Tsai,L.H.: Multi-sensory gamma stimulation ameliorates Alzheimer’s-associated pathology and improves cognition. Cell 177 (2), 256- 271 (2019)
|
[17] |
Shen,Q., Liu,L., Gu,X., Xing,D.: Photobiomodulation suppresses JNK3 by activation of ERK/MKP7 to attenuate AMPA receptor endocytosis in Alzheimer’s disease. Aging Cell 20 (1), e13289 (2020)
|
[18] |
Renier,N., Adams,E.L., Kirst,C., Wu,Z., Azevedo,R., Kohl,J., Autry,A.E., Kadiri,L., Venkataraju,K.U., Zhou,Y.: Mapping of brain activity by automated volume analysis of immediate early genes. Cell 165 (7), 1789- 1802 (2016)
|
[19] |
Renier,N., Adams,E.L., Kirst,C., Wu,Z., Azevedo,R., Kohl,J., Autry,A.E., Kadiri,L., Umadevi,V.K., Zhou,Y., Wang,V.X., Tang,C.Y., Olsen,O., Dulac,C., Osten,P., Tessier-Lavigne,M.: Mapping of brain activity by automated volume analysis of immediate early genes. Cell 165 (7), 1789- 1802 (2016)
|
[20] |
Bhattacharya,M., Dutta,A.: Computational modeling of the photon transport, tissue heating, and cytochrome C oxidase absorption during transcranial near-infrared stimulation. Brain Sci. 9 (8), 179 (2019)
|
[21] |
Lana,D., Ugolini,F., Giovannini,M.G.: Space-dependent glianeuron interplay in the hippocampus of transgenic models of β-amyloid deposition. Int. J. Mol. Sci. 21 (24), 9441 (2020)
|
[22] |
Mankin,E.A., Diehl,G.W., Sparks,F.T., Leutgeb,S., Leutgeb,J.K.: Hippocampal CA2 activity patterns change over time to a larger extent than between spatial contexts. Neuron 85 (1), 190- 201 (2015)
|
[23] |
Hainmueller,T., Bartos,M.: Dentate gyrus circuits for encoding, retrieval and discrimination of episodic memories. Nat. Rev. Neurosci. 21 (3), 153- 168 (2020)
|
[24] |
Le Merre,P., Ährlund-Richter,S., Carlén,M.: The mouse prefrontal cortex: Unity in diversity. Neuron 109 (12), 1925- 1944 (2021)
|
[25] |
Van Hoesen,G.W., Parvizi,J., Chu,C.: Orbitofrontal cortex pathology in Alzheimer’s disease. Cereb. Cortex 10 (3), 243- 251 (2000)
|
[26] |
Shi,T., Feng,S., Wei,M., Zhou,W.: Role of the anterior agranular insular cortex in the modulation of fear and anxiety. Brain Res. Bull. 155, 174- 183 (2020)
|
[27] |
Da Mesquita,S., Louveau,A., Vaccari,A., Smirnov,I., Cornelison,R.C., Kingsmore,K.M., Contarino,C., Onengut-Gumuscu,S., Farber,E., Raper,D., Viar,K.E., Powell,R.D., Baker,W., Dabhi,N., Bai,R., Cao,R., Hu,S., Rich,S.S., Munson,J.M., Lopes,M.B., Overall,C.C., Acton,S.T., Kipnis,J.: Functional aspects of meningeal lymphatics in ageing and Alzheimer’s disease. Nature 560 (7717), 185- 191 (2018)
|
[28] |
Liang,X., Luo,H.: Optical tissue clearing: illuminating brain function and dysfunction. Theranostics 11 (7), 3035- 3051 (2021)
|
[29] |
Ossenkoppele,R., Smith,R., Ohlsson,T., Strandberg,O., Mattsson,N., Insel,P.S., Palmqvist,S., Hansson,O.: Associations between tau, Aβ, and cortical thickness with cognition in Alzheimer disease. Neurology 92 (6), 601- 612 (2019)
|
[30] |
Li,D., Liu,S., Yu,T., Liu,Z., Sun,S., Bragin,D., Shirokov,A., Navolokin,N., Bragina,O., Hu,Z., Kurths,J., Fedosov,I., Blokhina,O., Dubrovski,A., Khorovodov,A., Terskov,A., Tzoy,M., Semyachkina-Glushkovskaya,O., Zhu,D.: Photostimulation of brain lymphatics in male newborn and adult rodents for therapy of intraventricular hemorrhage. Nat. Commun. 14, 6104 (2023)
|
[31] |
Huang,Z., Zhang,Y., Ma,X., Feng,Y., Zong,X., Jordan,J.D., Zhang,Q.: Photobiomodulation attenuates oligodendrocyte dysfunction and prevents adverse neurological consequences in a rat model of early life adversity. Theranostics 13 (3), 913- 930 (2023)
|
/
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